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Figure 3 in Species identification and seasonal prevalence of house dust mites in Assiut City, Egypt: A descriptive study in an urban area
Figure 3. Dermatophagoides farinae adult female (SEM photo) – a. Dorsal view shows sce (external scapular seta) is much longer than sci (internal scapular seta); b. Ventral view shows the genital system of the female; c. Lateral views shows the finely striated body and prodorsal shield; d. Hysterostoma region and anal opening; e. Epigynium and genital opening; f. Ventral view of the gnathostoma.
Figure 2 in Species identification and seasonal prevalence of house dust mites in Assiut City, Egypt: A descriptive study in an urban area
Figure 2. Dermatophagoides farinae (adult male) – a. Habitus (100×) before being cleared in Hoyer's medium and the enlarged 1st and 3rd pairs of legs are noted; b. Fused apodemes I (arrow) while apodemes II (arrow head) and apodemes III (curved arrow) are not fused (200×); c. Anal plate (arrow), post anal seta 2 (ps2) (curved arrow) (400×).
Figure 1 in Species identification and seasonal prevalence of house dust mites in Assiut City, Egypt: A descriptive study in an urban area
Figure 1. Dermatophagoides farinae (adult female) – a. Habitus (before being cleared) (10×); b. Habitus (after being cleared in Hoyer's medium) (x100); c. Distal solenidion on tarsus I (arrow head), terminal spinous process (curved arrow) and tarsus II with the two distal solenidia (arrow) (200×); d. Magnified tarsus II with distal solenidia (arrow head) and two small spinous tubercles (long arrow) (400×); e. The low-arched epigynium (arrow) and the faint transverse striations above it (arrow head); f. Bursa copulatrix (arrow), its external opening and sclerotized part (arrow head).
Figure 4 in Species identification and seasonal prevalence of house dust mites in Assiut City, Egypt: A descriptive study in an urban area
Figure 4. Dermatophagoides farinae adult male (SEM photo) – a. Ventral view showing the enlarged first pair of legs. B. The aedeagus; c. The anal plate containing the anal suckers.
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).
The Meltwater Pulse1A Triggered an Extreme Cooling Event: Evidence From Southern China. Meltwater Pulse Cooling Event (MCE). Winter temperature data during the last deglacial of Huguangyan Maar lake, Surface water temperature and seasonal diatom assemblage data of Huguangyan and Yunlong Lake.
<p>Here we present results of The lake averaged monthly mean surface water temperature over the period from September 2013 to August 2015 from Yunlong Tianchi Lake(YL)(25°52.2′N, 99°16.8′E, altitude: 2551 m a.s.l), southwestern China. The dataset include sediment trap main diatom percentages over the period from September 2013 to August 2015 from YL. Lake water temperature profiles at different depths (1, 3, 6, 9, 11, 13, 16 m) from November 2008 to May 2009 in Huguang Maar Lake (HML)(21°9′N, 110°17′E), Southern China. AMS radiocarbon dates of plant remains and bulk sediment samples for Huguangyan Maar Lake over the last ~17 cal ka BP. The main diatom assemblage percentages (%) from 17 to 10 cal ka BP at Huguangyan Maar Lake. Diatom-based reconstruction of winter temperature (WT) from 17 to 10 cal ka BP at Huguangyan Maar Lake.</p>
Fig. 6 in Croton sertanejus, a new species from Seasonally Dry Tropical Forest in Brazil, and redescription of C. echioides (Euphorbiaceae)
Fig. 6. Cross sections of the leaf blade of C. echioides Baill. (A, E–I, N–Q) and C. sertanejus Sodré & M.J.Silva sp. nov. (B–D, J–M, R–V). A. Median portion of the leaf blade of C. echioides, note the stipitate trichomes of abaxial surface in lateral view. B. Median portion of the leaf blade of C. sertanejus, note the sessile trichomes of abaxial surface in lateral view. C. Leaf margin of C. sertanejus, note simple trichomes of adaxial surface. D. Base of the trichome of adaxial surface of C. sertanejus. E. Vascular bundle of C. echioides. F–H. Median portion of the leaf blade of C. echioides. I. Leaf margin of C. echioides. J. Vascular bundle of C. sertanejus. K–L. Median portion of the leaf blade of C. sertanejus. M. Leaf margin of C. sertanejus. N. Primary vein of C. echioides. O. Detail of vascular cylinder of C. echioides primary vein. P. Collenchyma in adaxial surface of C. echioides primary vein. Q. Detail of the vascular bundle, note xylem, phloem, laticifer and druse. R. Primary vein of C. sertanejus. S. Detail of vascular cylinder of C. sertanejus primary vein. T. Collenchyma in adaxial surface of C. echioides primary vein. U. Detail of the epidermis and cortex of C. echioides primary vein. V. Detail of the vascular bundle, note xylem, phloem and druse. Arrowheads indicate stomata; asterisks indicate laticifers. Abbreviations: cl = collenchyma; co = cortex; d = druses; ep = epidermis; i = idioblasts; pa = ground parenchyma; ph = phloem; pp = palisade parenchyma; sp = spongy parenchyma; st = simple trichome; stt = stellate trichome; vb = vascular bundle; vc = vascular cylinder; xy = xylem. A, E–I, N–Q = R.C. Sodré et al. 3284 (BOTU); B–D, J–M, R–V = R.C. Sodré et al. 3350, holotype (BOTU). Scale bars: A–C, N, R = 200 µm; D–G, I–M, P–Q, T–V = 50 µm; H = 20 µm; O, S = 100 µm.
Fig. 1 in Croton sertanejus, a new species from Seasonally Dry Tropical Forest in Brazil, and redescription of C. echioides (Euphorbiaceae)
Fig. 1. Croton sertanejus Sodré & M.J.Silva sp. nov. A. Flowering branch. B. Detail of older portion of stem with leaf scars. C 1 –C 2. Indumentum of the stems. C 1. Tomentose indumentum. C 2. Hirsute indumentum. D 1 –D 3. Trichomes of the stems. D 1. Stellate trichome. D 2. Multiradiate-porrect trichome. D 3. Stellate-porrect trichome. E. Stipule, ventral surface. F 1 –F 2. Leaves. F 1. Elliptic leaf blade. F 2. Ovate leaf blade. G. Detail of the galls on the leaf blade. H. Extrafloral nectaries of leaf base in adaxial view. I. Colleters of leaf margin in adaxial view. J1–J3. Indumentum of leaf blades. J1. Tomentose indumentum of abaxial surface. J2. Sparse indumentum of simple, stellate-porrect or 2-radiate trichomes of adaxial surface. J 3. Sparse indumentum of stellate trichomes of adaxial surface. K. Inflorescence. L 1. Staminate flower bract, ventral surface. L 2. Staminate flower bracteole, ventral surface. M. Staminate flower. N 1 – N 3. Lobes of staminate flower calyx in dorsal view. N 1. Two lobes showing the union of the calyx. N 2. Dense indumentum of stellate-porrect trichomes. N3. Sparse indumentum of stellate-porrect trichomes. O 1 –O 2. Pistillate flower petals in dorsal view. O 1. Obovate petal. O 2. Oblanceolate petal. P. Stamen. Q 1. Pistillate flower bract, ventral surface. Q 2. Pistillate flower bracteole, ventral surface. R. Pistillate flower. S 1 –S 2. Pistillate flower sepal. S 1. Dorsal view. S 2. Ventral view. T. Gynoecium. U. Nectary disk and reduced petals of the pistillate flowers (cut out sepals and gynoecium removed). V. Fruit. W 1. Fruit columella. W2. Apex of columella with irregular and plane tips. W3. Apex of columella with three slightly ascending tips. X 1. Seed, dorsal side. X2. Seed, ventral side. Drawing by Renato Galhardo: A–U = R.C. Sodré et al. 3350, holotype (BOTU); V–X = K.N.C. Castro & J.B.A. Souza 471 (CEN).
Fig. 4. Croton echioides Baill. A. Flowering branch. B in Croton sertanejus, a new species from Seasonally Dry Tropical Forest in Brazil, and redescription of C. echioides (Euphorbiaceae)
Fig. 4. Croton echioides Baill. A. Flowering branch. B. Detail of the indumentum of the stems and stipule. C 1 –C 2. Trichomes of the stems. C 1. Stellate-rotate trichome. C 2. Stellate-porrect trichome. D 1 –D 2. Stipules. D1. Surface. D 2. Ventral surface. E 1–E3. Leaves, note the variation in the shape of the leaf blades and in the length of the petioles. F1–F3. Extrafloral nectaries of leaf base in abaxial view. F1. Stipitatepatelliform. F 2. Obconic. F 3. Cylindric. G. Colleters of leaf margin in adaxial view. H 1. Leaf indumentum of the abaxial surface. H 2. Leaf indumentum of the adaxial surface. I. Inflorescence. J 1. Staminate flower bract, ventral surface. J 2. Staminate flower bracteole, ventral surface. K. Staminate flower. L 1 –L 2. Lobes of staminate flower calyces in dorsal view. L1. Dense indumentum. L2. Sparse indumentum. M1–M2. Staminate flower petals in dorsal view. M1. Obovate petal. M2. Oboval-oblanceolate petal. N. Stamen. O 1. Pistillate flower bract, ventral surface. O 2 –O 3. Pistillate flower bracteoles, ventral surface. P. Pistillate flower. Q. Pistillate flower in upper view showing ventral surface of the sepals, disk and reduced petals (gynoecium removed), note the unequal sepals. R 1 –R 2. Indumentum of ventral surface of the pistillate flower sepals. S. Pistillate flower in lower view showing dorsal surface of sepals. T. Indumentum of dorsal surface of the pistillate flower sepals. U. Gynoecium. V. Nectary disk and reduced petals of the pistillate flowers (cut out sepals and gynoecium removed). W. Fruit. X 1. Fruit columella. X 2. Apex of columella with plane tips. X 3. Apex of columella with three slightly ascending tips. Y 1. Seed, dorsal side. Y 2. Seed, ventral side. Drawing by Renato Galhardo: A, E2, F1 = E. Melo et al. 7571 (HUEFS); E1, F3, O1–V = R.C. Sodré et al. 3284 (BOTU); B–D2, G–N = R.C. Sodré et al. 3314 (BOTU); E3, F2, W–Y2 = V.C. Souza et al. 5495 (ESA).
Supplementary data: Modelling of future changes in seasonal snowpack and impacts on summer low flows in Alpine catchments
<p>The files in this record represent supplementary data for the article titled “Modelling of future changes in seasonal snowpack and impacts on summer low flows in Alpine catchments” in Water Resources Research. The files contain simulations of the HBV rainfall-runoff model for 14 alpine catchments in Switzerland. The model simulated different water balance components (such as runoff, snow water equivalent and evapotranspiration) for the reference period 1980-2009 and the three scenario periods (2020-2049, 2045-2074 and 2070-2099) using the A1B emission scenario.</p>
Fig. 6 Seasonal parasite transmission along the lower Mbam river showing a in ONCHOCERCA VOLVULUS transmission in the Mbam valley of Cameroon following 16 years of annual community-directed treatment with ivermectin, and the description of a new cytotype of SIMULIUM SQUAMOSUM
Fig. 6 Seasonal parasite transmission along the lower Mbam river showing a combined parity and infection rates for flies dissected at Bayomen and Nyamongo I riverside sites (L1–L2 = percentage of flies infected with developing parasite stages only, L3H = percentage of flies containing L3 stages in the head), and b monthly transmission potentials at Bayomen, Nyamongo I, and Egona II estimated based on dissection data only. Ondouano not shown since no larvae were found in dissected flies
Рис. 7. Сезонная Δинамика соΔержимого цист H. glycines Fig. 7. Seasonal dynamics of H. glycines cysts content in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions
Рис. 7. Сезонная Δинамика соΔержимого цист H. glycines Fig. 7. Seasonal dynamics of H. glycines cysts content
Рис. 8. Изменение жизнеспособности цист Heterodera glycines на протяжении сезона размножения Fig. 8. Changes in the viability of Heterodera glycines cysts during the breeding season in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions
Рис. 8. Изменение жизнеспособности цист Heterodera glycines на протяжении сезона размножения Fig. 8. Changes in the viability of Heterodera glycines cysts during the breeding season
Рис. 4. Сезонная Δинамика размеров цист Heterodera glycines и чисΛа яиц в них. Размер цист в баΛΛах: 1 — меΛкие, 2 — среΔние, 3 — крупные Fig. 4. Seasonal dynamics of the size of Heterodera glycines cysts and the number of eggs in them. The size of cysts in classes: 1 — small, 2 — medium, 3 — large in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions
Рис. 4. Сезонная Δинамика размеров цист Heterodera glycines и чисΛа яиц в них. Размер цист в баΛΛах: 1 — меΛкие, 2 — среΔние, 3 — крупные Fig. 4. Seasonal dynamics of the size of Heterodera glycines cysts and the number of eggs in them. The size of cysts in classes: 1 — small, 2 — medium, 3 — large
FIGURE 3 in A new species of the seasonal killifish genus Moema (Cyprinodontiformes: Rivulidae) from the Piraí watershed in the Southwest Amazon basin
FIGURE 3 | Moema juanderibaensis, MNKP 16543, paratype, female, 36.1 mm SL (1 day after collection, left side), Bolivia, Santa Cruz, Santa Rosa del Sara.
FIGURE 6 in A new species of the seasonal killifish genus Moema (Cyprinodontiformes: Rivulidae) from the Piraí watershed in the Southwest Amazon basin
FIGURE 6 | Occurrence localities of Moema species in Bolivia and surroundings. Sources: Hydrologic Units from Lehner, Grill (2013); Basemap ESRI World Topo (2022).
FIGURE 2 in A new species of the seasonal killifish genus Moema (Cyprinodontiformes: Rivulidae) from the Piraí watershed in the Southwest Amazon basin
FIGURE 2 | Moema juanderibaensis, MNKP 16539, holotype, male, 41.9 mm SL (2 days after collection, right side), Bolivia, Santa Cruz, Santa Rosa del Sara.
FIGURE 4 in A new species of the seasonal killifish genus Moema (Cyprinodontiformes: Rivulidae) from the Piraí watershed in the Southwest Amazon basin
FIGURE 4 | Moema juanderibaensis, MNKP 16541, paratypes, males, 41.3–46.1 mm SL (2 days after collection, left side), Bolivia, Santa Cruz, Santa Rosa del Sara.
FIGURE 1 in A new species of the seasonal killifish genus Moema (Cyprinodontiformes: Rivulidae) from the Piraí watershed in the Southwest Amazon basin
FIGURE 1 | Moema juanderibaensis, MNKP 16539, holotype, male, 41.9 mm SL (24 days after collection, left side), Bolivia, Santa Cruz, Santa Rosa del Sara.
FIGURE 7 in A new species of the seasonal killifish genus Moema (Cyprinodontiformes: Rivulidae) from the Piraí watershed in the Southwest Amazon basin
FIGURE 7 | Moema pepotei, CAS-SU 63604, holotype, male, 45.4 mm SL, Brazil, Rondônia, Forte Príncipe da Beira (on Bolivian border). Source: CAS Ichthyology Primary Types Imagebase.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.